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The Other Side of Fear: Tips For Traveling as a Special Needs Family

This post is sponsored be Alaska Airlines. I’m so excited to be partnering with Alaska Airlines this year as we’ve got some exciting things planned. Thank you so much for supporting sponsors here on TLM, as it allows me to keep creating content I care about. As always, all opinions are my own. ***** Fear...

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Summertime and the Living’s easy

Miggy’s Summer survival guide: 1. Good tunes. 2. Flying by the seat of our pants. You’re welcome. **** Memorial Day started our summer off right and I’m thinking it’s all because of our amazing lack of  planning. My husband had just gotten back in town Sunday afternoon, a couple of the girls had been sick,...

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Special Needs Spotlight || William

Hi, I’m Elizabeth Reynolds! I am mom to William Reynolds and co-Founder of The Champ Foundation. William was diagnosed with Pearson Syndrome when he was 2 months old. Pearson Syndrome is a mitochondrial deletion disorder. Most children with Pearson Syndrome do not live past their third birthday. When William was born, there was no research...

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Some Americans in Paris

The husband and I are going to Paris in a few weeks and (this seems strange to say) I’ve barely thought about it at all! But now that it’s getting closer and closer I’m sorta like wait… I’m going to Paris in a few weeks!! While I am really, really excited for Paris, this will...

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Special Needs Spotlight || Elise

Thank you so much for having me, Miggy! My name is Elise and I’m 15 years old. I live in Minnesota with my parents, older brother, and identical twin sister. I’m also the owner of a handmade children’s clothing shop, Baby Buffalo Co. I have PANDAS, which stands for Pediatric Autoimmune Neuropsychiatric Disorder Associated with...

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Color Your Own

Thanks to Hi Little One for sponsoring today’s post and thanks to my readers for supporting sponsors here at This Little Miggy so I can keep creating content I love. As always, all opinions are my own! I love creating and crafting with my kids. As an artist I want them to have a love...

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Special Needs Spotlight || Kuba

Miggy: Welcome Cydney! So happy to have you here today sharing your beautiful family with us, especially your son Kuba. Let’s start at the beginning, can you take me back to the day you knew Kuba would have special needs? Was this in utero, shortly after birth or sometime after that? Do you remember how...

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Hey, I'm Amy!

I'm an author, artist, and disability advocate. I live with my handsome husband and three beautiful daughters in Cincinnati, Ohio.

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